45 results · 21ms · Sources: EU EUDAMED, US FDA

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REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESH

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MIS IMPLANT SYSTEM DECIVE

FDA 510(k)
FDA Class 2 ·Dental

PASS SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 29, 2011

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVY·April 9, 2013

SOLETRA

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·March 25, 2011

FLEXTEND IS-1 BI POSITIVE FIX

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code DTB·May 8, 2008

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 6, 2010

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 12, 2011

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 2, 2011

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 25, 2011

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 10, 2011

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·September 27, 2010

OT ULTRA TEST STRIPS

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 5, 2012

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 11, 2011

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 11, 2011

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 11, 2011

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 11, 2011

ISODUR PROSTHESIS HEAD 12/14 28MM M

FDA Adverse Event
Malfunction ·AESCULAP AG AND CO. KG·Product code LPH·January 16, 2015